CN104842617A - High-water-vapor-barrier polyvinylidene fluoride film and preparation method thereof - Google Patents

High-water-vapor-barrier polyvinylidene fluoride film and preparation method thereof Download PDF

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CN104842617A
CN104842617A CN201510252483.9A CN201510252483A CN104842617A CN 104842617 A CN104842617 A CN 104842617A CN 201510252483 A CN201510252483 A CN 201510252483A CN 104842617 A CN104842617 A CN 104842617A
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butyl
hydroxyl
water vapor
polyvinylidene fluoride
phenyl
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CN104842617B (en
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王同心
陈坤
金鹰
沈一春
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Zhongtian Photovoltaic Materials Co ltd
Jiangsu Zhongtian Technology Co Ltd
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Zhongtian Technology Advanced Materials Co ltd
Jiangsu Zhongtian Technology Co Ltd
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    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B27/00—Layered products comprising a layer of synthetic resin
    • B32B27/06—Layered products comprising a layer of synthetic resin as the main or only constituent of a layer, which is next to another layer of the same or of a different material
    • B32B27/08—Layered products comprising a layer of synthetic resin as the main or only constituent of a layer, which is next to another layer of the same or of a different material of synthetic resin
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29D—PRODUCING PARTICULAR ARTICLES FROM PLASTICS OR FROM SUBSTANCES IN A PLASTIC STATE
    • B29D7/00—Producing flat articles, e.g. films or sheets
    • B29D7/01—Films or sheets
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B27/00—Layered products comprising a layer of synthetic resin
    • B32B27/18—Layered products comprising a layer of synthetic resin characterised by the use of special additives
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B27/00—Layered products comprising a layer of synthetic resin
    • B32B27/18—Layered products comprising a layer of synthetic resin characterised by the use of special additives
    • B32B27/20—Layered products comprising a layer of synthetic resin characterised by the use of special additives using fillers, pigments, thixotroping agents
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B27/00—Layered products comprising a layer of synthetic resin
    • B32B27/30—Layered products comprising a layer of synthetic resin comprising vinyl (co)polymers; comprising acrylic (co)polymers
    • B32B27/304—Layered products comprising a layer of synthetic resin comprising vinyl (co)polymers; comprising acrylic (co)polymers comprising vinyl halide (co)polymers, e.g. PVC, PVDC, PVF, PVDF
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
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    • C08K3/18—Oxygen-containing compounds, e.g. metal carbonyls
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    • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K3/00—Use of inorganic substances as compounding ingredients
    • C08K3/18—Oxygen-containing compounds, e.g. metal carbonyls
    • C08K3/24—Acids; Salts thereof
    • C08K3/26—Carbonates; Bicarbonates
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00—Use of organic ingredients
    • C08K5/04—Oxygen-containing compounds
    • C08K5/13—Phenols; Phenolates
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00—Use of organic ingredients
    • C08K5/16—Nitrogen-containing compounds
    • C08K5/34—Heterocyclic compounds having nitrogen in the ring
    • C08K5/3467—Heterocyclic compounds having nitrogen in the ring having more than two nitrogen atoms in the ring
    • C08K5/3472—Five-membered rings
    • C08K5/3475—Five-membered rings condensed with carbocyclic rings
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    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00—Use of organic ingredients
    • C08K5/36—Sulfur-, selenium-, or tellurium-containing compounds
    • C08K5/37—Thiols
    • C08K5/375—Thiols containing six-membered aromatic rings
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L27/00—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers
    • C08L27/02—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers not modified by chemical after-treatment
    • C08L27/12—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers not modified by chemical after-treatment containing fluorine atoms
    • C08L27/16—Homopolymers or copolymers or vinylidene fluoride
    • B—PERFORMING OPERATIONS; TRANSPORTING
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    • B32B2250/00—Layers arrangement
    • B32B2250/24—All layers being polymeric
    • B32B2250/246—All polymers belonging to those covered by groups B32B27/32 and B32B27/30
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B2307/00—Properties of the layers or laminate
    • B32B2307/70—Other properties
    • B32B2307/724—Permeability to gases, adsorption
    • B32B2307/7242—Non-permeable
    • B32B2307/7246—Water vapor barrier
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B2457/00—Electrical equipment
    • B32B2457/12—Photovoltaic modules
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
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    • C08K3/00—Use of inorganic substances as compounding ingredients
    • C08K3/18—Oxygen-containing compounds, e.g. metal carbonyls
    • C08K3/20—Oxides; Hydroxides
    • C08K3/22—Oxides; Hydroxides of metals
    • C08K2003/2237—Oxides; Hydroxides of metals of titanium
    • C08K2003/2241—Titanium dioxide
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K3/00—Use of inorganic substances as compounding ingredients
    • C08K3/18—Oxygen-containing compounds, e.g. metal carbonyls
    • C08K3/24—Acids; Salts thereof
    • C08K3/26—Carbonates; Bicarbonates
    • C08K2003/265—Calcium, strontium or barium carbonate
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K2201/00—Specific properties of additives
    • C08K2201/014—Additives containing two or more different additives of the same subgroup in C08K
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2203/00—Applications
    • C08L2203/16—Applications used for films
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2203/00—Applications
    • C08L2203/20—Applications use in electrical or conductive gadgets
    • C08L2203/204—Applications use in electrical or conductive gadgets use in solar cells

Abstract

The invention relates to a high-water-vapor-barrier polyvinylidene fluoride film and a preparation method thereof. The high-water-vapor-barrier polyvinylidene fluoride film comprises a polyvinylidene fluoride layer and a water vapor barrier layer, wherein the water vapor barrier layer is compounded on one side of the polyvinylidene fluoride layer. The high-water-vapor-barrier polyvinylidene fluoride film is prepared by multilayer coextrusion or multilayer co-blowing of thermoplastic materials. The preparation method comprises the following steps: and respectively mixing the raw materials of the polyvinylidene fluoride layer and the water vapor barrier layer at a high speed, and then respectively putting the raw materials into a double-screw extruder for extrusion to respectively obtain raw material particles of the polyvinylidene fluoride layer and the water vapor barrier layer. And respectively putting raw material particles of the polyvinylidene fluoride layer and the water vapor barrier layer into two extruders, melting and plasticizing, extruding and converging the raw material particles in a T-shaped die head, and extruding through a die gap. Cooling and shaping the extrudate by a cooling roller, carrying out heat treatment and recovery shaping on the cooled film by a hot air drying tunnel, cutting edges, and rolling to obtain the required film.

Description

A kind of high water vapor rejection polyvinylidene difluoride film and preparation method thereof
Technical field
What the present invention relates to is Material Field, particularly composite, specifically refers to a kind of high water vapor rejection polyvinylidene difluoride film and preparation method thereof.
Background technology
The PID phenomenon of photovoltaic module has caused the great attention of whole photovoltaic industry, and increasing assembly manufacturer and related research institutes conduct extensive research the induction mechanism that assembly PID decays and analyze.Affect primary outer that assembly PID decays because have environment temperature, ambient humidity, and system voltage is at alloy frame, the biasing electric field that formed between glass and internal circuit.Find in the process to photovoltaic plant long-term observation, when assembly surface remain morning dew or rainwater and have illumination, the most easily there is PID phenomenon.According to current study mechanism of decaying to assembly PID, the infiltration of steam is the major inducing factor that PID decay occurs assembly.
Solar energy backboard is the important assembly of of solar panel; solar cell backboard plays a part cell piece in protection photovoltaic module; prevent the dust in air and moisture (especially overcast and rainy moisture) from can enter into inner side through solar energy backboard; the infiltration of water vapour can have influence on the performance of adhesive linkage and cause backboard to be peeled off; and then make more moistures directly contact cell piece and make cell piece oxidized, cause scrapping of solar cell.The backboard generally conventional three-decker (PVDF or PVF/PET/PVDF or PVF) of solar module encapsulation; wherein; outer protective layer PVDF (PVF) has good environment resistant erosiveness; intermediate layer is that PET polyester film has good insulating properties, and internal layer PVDF (PVF) need through surface treatment to have good adhesive property.
Such as, Chinese patent application 201010022009.4 discloses a kind of back veneer material of solar module back-protective layer.This special back seal film for solar cell is the composite membrane be made up of through vacuum hotpressing lamination three layer laminated film materials, and this three layer laminated films material is: outer is one of llowing group of materials: polyvinyl fluoride, Kynoar, fluoroplastics, ethene one chlorotrifluoroethylene or ethylene propylene diene rubber; Middle level is one of llowing group of materials: ethene-vinylacetate or epoxy resin; Internal layer is PETG.The back veneer material of this application has good air exclusion performance, good anti-oxidation and moisture resistant performance, good electrical insulation capability, can prevent the performance of the hydrolysis of binding for a long time.
In prior art, the needs of solar cell backboard have lower water vapor transmittance, thus form good protective effect to cell piece.The water vapor barrier property of backboard product mainly relies on PET in the market, but aging and hydrolysis can occur gradually PET in Long-Time Service process, and the water vapor barrier property of PVDF and PVF is poor, and its water vapor transmittance is all at 25g/(m 2* 24h) more than (test condition is 38 DEG C, 100%RH), be difficult to provide good water vapor rejection.Therefore need the water vapor barrier property improving PVDF thin film further, to improve the water vapor barrier property of backboard, thus improve the anti-PID performance of assembly.
Summary of the invention
The present invention seeks to provide a kind of high water vapor rejection polyvinylidene difluoride film and preparation method thereof for above-mentioned weak point, a kind of existing good water vapor rejection performance, solar cell backboard polyvinylidene difluoride film having again good weatherability properties and preparation method thereof.
A kind of high water vapor rejection polyvinylidene difluoride film of the present invention and preparation method thereof realizes by the following technical solutions:
A kind of high water vapor rejection polyvinylidene difluoride film comprises polyvinylidene fluoride layer and aqueous vapor separation layer, and the side of described polyvinylidene fluoride layer is compounded with aqueous vapor separation layer.
High water vapor rejection polyvinylidene difluoride film of the present invention adopts thermoplastic mode that is multi-layer co-extruded or the common blown film of multilayer to prepare.
The thickness of described polyvinylidene fluoride layer is 5-45 micron, and described water vapor rejection layer thickness is 5-45 micron.
Described polyvinylidene fluoride layer comprises the raw material of following mass parts: Kynoar 60-90 part, plasticity resin 0.1-30 part, inorganic filler 0.1-15 part, antioxidant 0.1-3 part, anti ultraviolet agent 0.1-3 part.
Described Kynoar molecular weight is 20-100 ten thousand, and molecular weight distribution width is 1.1-2.
Described plasticity resin is one or more the combination in esters of acrylic acid, methacrylate-based resin class.
In described polyvinylidene fluoride layer, inorganic filler is one or more the combination in titanium dioxide, talcum powder, silica, imvite.
In described polyvinylidene fluoride layer, antioxidant is three (3, 5-di-t-butyl-4-hydroxybenzyl) isocyanuric acid ester, triethylene glycol-bis--[3-(3-tertiary butyl-4-hydroxy-5-aminomethyl phenyl) propionic ester], 2, 2 '-di-2-ethylhexylphosphine oxide-(4-methyl-6-tert-butylphenol, 4-4 '-thiobis-(3-methyl-6-tert-butyl phenol), 4-4 '-butyl is two-and (3-methyl-6-tert-butyl phenol), decanedioic acid two (2, 2, 6, 6-tetramethyl-4-piperidyl) ester, tricresyl phosphite (1, 2, 2, 6, 6-pentamethyl-4-piperidyl) ester, poly-[(1-(β-ethyl)-2, 2, 6, 6-tetramethyl-4-piperidyl) succinic acid], poly-{ [6-[(1, 1, 3, 3-tetramethyl butyl)-imino group]-1, 3, 5-triazine-2, 4-bis-base], [2-(2, 2, 6, 6-tetramethyl-4-piperidyl)-secondary amino]-hexa-methylene-[4-(2, 2, 6, 6-tetramethyl-4-piperidyl)-secondary amino] in one or more combination.
In described polyvinylidene fluoride layer, anti ultraviolet agent is 2,2 '-dihydroxy-4,4 '-dimethoxy-benzophenone, 2-hydroxyl-5-chlorobenzophenone, 2-(2 '-hydroxyl-5 '-tert-butyl-phenyl) BTA, 2-(2 '-hydroxyl-5 '-aminophenyl) BTA, salicyl salicylate (salsalate) bisphenol-A ester, 2-(2-hydroxyl-3,5-di-tert-pentyl-phenyl) BTA, 2,2 '-(Isosorbide-5-Nitrae-phenylene) two-4H-3,1-benzoxazine-4-ketone, 2-(2 '-hydroxyl-3 ', 5 '-3,5-dimethylphenyl) BTA, 2-(2 '-methyl-4 '-hydroxy phenyl) BTA, two-(2-methoxyl group-4-hydroxyl-5-benzoylphenyl) methane, 2-(2 '-hydroxy-5-methyl base phenyl) BTA, 2-(2 '-hydroxyl-5-aminomethyl phenyl)-5-butyl ester BTA, 2-hydroxyl-4-alkoxy benzophenone, 3,5-di-t-butyl-4-hydroxyl-benzoic acid cetyl ester, three (1,2,2,6,6-pentamethyl-4-piperidyl) phosphite ester, two-2,2,6, the 6-tetramethyl piperidine alcohol esters of decanedioic acid, the polymer of succinic acid and 4-hydroxyl-2,2,6,6-tetramethyl-1-piperidine alcohols, N, N ' polymer of amino-1,3, the 5-triazine of-bis-(2,2,6,6-tetramethyl-4-piperidyl)-1,6-hexamethylene diamine and the chloro-6-of 2,4-bis-(1,1,3,3-tetramethyl butyl), N, N '-bis-(2,2,6,6-tetramethyl-4-piperidyl)-1,6-hexamethylene diamine and the chloro-6-of 2,4-bis-(4-morpholinyl)-1,3,5-triazines polymer in one or more combination.
Described aqueous vapor separation layer comprises the raw material of following mass parts: polyvinylidene chloride 70-100 part, inorganic filler 1-20 part, antioxidant 0.5-3 part, anti ultraviolet agent 0.5-3 part.
In described aqueous vapor separation layer, inorganic filler is one or more the combination in titanium dioxide, talcum powder, imvite, silica, calcium carbonate.
In described aqueous vapor separation layer, antioxidant is 2, 6-di-t-butyl-4-methylphenol, n-octadecane base-3-(3 ', 5 '-two tertiary Ding-4 '-hydroxy phenyl) propionic ester, four-[methylene-3-(3 ', 5 '-di-t-butyl-4-hydroxy phenyl) propionic ester] methane, three (3, 5-di-t-butyl-4-hydroxybenzyl) isocyanuric acid ester, triethylene glycol-bis--[3-(3-tertiary butyl-4-hydroxy-5-aminomethyl phenyl) propionic ester], 2, 2 '-di-2-ethylhexylphosphine oxide-(4-methyl-6-tert-butylphenol, 4-4 '-thiobis-(3-methyl-6-tert-butyl phenol), 4-4 '-butyl is two-and (3-methyl-6-tert-butyl phenol), decanedioic acid two (2, 2, 6, 6-tetramethyl-4-piperidyl) ester, tricresyl phosphite (1, 2, 2, 6, 6-pentamethyl-4-piperidyl) ester, poly-[(1-(β-ethyl)-2, 2, 6, 6-tetramethyl-4-piperidyl) succinic acid], poly-{ [6-[(1, 1, 3, 3-tetramethyl butyl)-imino group]-1, 3, 5-triazine-2, 4-bis-base], [2-(2, 2, 6, 6-tetramethyl-4-piperidyl)-secondary amino]-hexa-methylene-[4-(2, 2, 6, 6-tetramethyl-4-piperidyl)-secondary amino] in one or more combination.
In described aqueous vapor separation layer, anti ultraviolet agent is 2-(2-hydroxyl-5-aminomethyl phenyl)-BTA, 2-[2-hydroxyl-3, 5-(a, a-dimethyl-benzyl-) phenyl]-BTA, 2-(2-hydroxyl-{ 3, 5-tert-butyl-phenyl)-BTA, 2-(2-hydroxyl-3, 5-butyl-5-aminomethyl phenyl)-5 chlorobenzotriazoles, 2-(2-hydroxyl-3, 5-tert-butyl-phenyl)-5-chlorobenzotriazole, 2-(2-hydroxyl-3, 5-bis--tertiary pentyl phenyl)-BTA, 2-(2-hydroxyl-5-tert-butyl-phenyl)-BTA, one or more combination in 2-(2-hydroxyl-3-sec-butyl-5-tert-butyl-phenyl)-BTA and 2-(the tertiary octyl phenyl of 2-hydroxyl-5-)-BTA.
A kind of preparation method of high water vapor rejection polyvinylidene difluoride film takes following steps:
Respectively by polyvinylidene fluoride layer and aqueous vapor separation layer raw material after 15-40 DEG C of mixed at high speed, to put in double screw extruder 150-220 DEG C respectively and extrude, obtain the raw material particle of polyvinylidene fluoride layer and aqueous vapor separation layer respectively.
Polyvinylidene fluoride layer and aqueous vapor separation layer raw material particle are put in two extruders respectively, at 180-220 DEG C, carries out melting, plasticizing, extrude and conflux in T-shaped die head, being extruded at 190-210 DEG C by die slot.Extrudate carries out cooling and shaping through the chill roll of-20-10 DEG C, and cooled film heat-treats reply sizing, rolling after trimming through the hot blast drying tunnel of 0-50 DEG C, thus obtains required high water vapor rejection polyvinylidene difluoride film.
Compared with prior art, the invention has the beneficial effects as follows: a kind of high water vapor rejection polyvinylidene difluoride film of the present invention and preparation method thereof, a kind of existing good water vapor rejection performance, solar cell backboard polyvinylidene difluoride film having again good weatherability properties and preparation method thereof.The aqueous vapor separation layer that the present invention introduces, can improve the water vapor rejection character of PVDF thin film, its water vapor transmittance is at 3g/(m 2* 24h) (test condition is 38 DEG C, 100%RH) below.Compared with prior art, the backboard of this PVDF thin film compound is used to have lower water vapor transmittance, and the solar module using the backboard product of this PVDF thin film to encapsulate, when carrying out PID test, component power decay is within 2%.
Accompanying drawing explanation
Below with reference to accompanying drawing, the present invention is described in further detail:
Fig. 1 is a kind of high water vapor rejection polyvinylidene difluoride film structural representation.
Detailed description of the invention
With reference to accompanying drawing 1, a kind of high water vapor rejection polyvinylidene difluoride film comprises polyvinylidene fluoride layer 1 and aqueous vapor separation layer 2, and the side of described polyvinylidene fluoride layer 1 is compounded with aqueous vapor separation layer 2.
High water vapor rejection polyvinylidene difluoride film of the present invention adopts thermoplastic mode that is multi-layer co-extruded or the common blown film of multilayer to prepare.
Described polyvinylidene fluoride layer 1 thickness is 5-45 micron, and described water vapor rejection layer thickness 2 is 5-45 micron.
Described polyvinylidene fluoride layer 1 comprises the raw material of following mass parts: Kynoar 60-90 part, plasticity resin 0.1-30 part, inorganic filler 0.1-15 part, antioxidant 0.1-3 part, anti ultraviolet agent 0.1-3 part.
Described Kynoar molecular weight is 20-100 ten thousand, and molecular weight distribution width is 1.1-2.
Described plasticity resin is one or more the combination in esters of acrylic acid, methacrylate-based resin class.
In described polyvinylidene fluoride layer 1, inorganic filler is one or more the combination in titanium dioxide, talcum powder, silica, imvite.
In described polyvinylidene fluoride layer 1, antioxidant is three (3, 5-di-t-butyl-4-hydroxybenzyl) isocyanuric acid ester, triethylene glycol-bis--[3-(3-tertiary butyl-4-hydroxy-5-aminomethyl phenyl) propionic ester], 2, 2 '-di-2-ethylhexylphosphine oxide-(4-methyl-6-tert-butylphenol, 4-4 '-thiobis-(3-methyl-6-tert-butyl phenol), 4-4 '-butyl is two-and (3-methyl-6-tert-butyl phenol), decanedioic acid two (2, 2, 6, 6-tetramethyl-4-piperidyl) ester, tricresyl phosphite (1, 2, 2, 6, 6-pentamethyl-4-piperidyl) ester, poly-[(1-(β-ethyl)-2, 2, 6, 6-tetramethyl-4-piperidyl) succinic acid], poly-{ [6-[(1, 1, 3, 3-tetramethyl butyl)-imino group]-1, 3, 5-triazine-2, 4-bis-base], [2-(2, 2, 6, 6-tetramethyl-4-piperidyl)-secondary amino]-hexa-methylene-[4-(2, 2, 6, 6-tetramethyl-4-piperidyl)-secondary amino] in one or more combination.
In described polyvinylidene fluoride layer 1, anti ultraviolet agent is 2,2 '-dihydroxy-4,4 '-dimethoxy-benzophenone, 2-hydroxyl-5-chlorobenzophenone, 2-(2 '-hydroxyl-5 '-tert-butyl-phenyl) BTA, 2-(2 '-hydroxyl-5 '-aminophenyl) BTA, salicyl salicylate (salsalate) bisphenol-A ester, 2-(2-hydroxyl-3,5-di-tert-pentyl-phenyl) BTA, 2,2 '-(Isosorbide-5-Nitrae-phenylene) two-4H-3,1-benzoxazine-4-ketone, 2-(2 '-hydroxyl-3 ', 5 '-3,5-dimethylphenyl) BTA, 2-(2 '-methyl-4 '-hydroxy phenyl) BTA, two-(2-methoxyl group-4-hydroxyl-5-benzoylphenyl) methane, 2-(2 '-hydroxy-5-methyl base phenyl) BTA, 2-(2 '-hydroxyl-5-aminomethyl phenyl)-5-butyl ester BTA, 2-hydroxyl-4-alkoxy benzophenone, 3,5-di-t-butyl-4-hydroxyl-benzoic acid cetyl ester, three (1,2,2,6,6-pentamethyl-4-piperidyl) phosphite ester, two-2,2,6, the 6-tetramethyl piperidine alcohol esters of decanedioic acid, the polymer of succinic acid and 4-hydroxyl-2,2,6,6-tetramethyl-1-piperidine alcohols, N, N ' polymer of amino-1,3, the 5-triazine of-bis-(2,2,6,6-tetramethyl-4-piperidyl)-1,6-hexamethylene diamine and the chloro-6-of 2,4-bis-(1,1,3,3-tetramethyl butyl), N, N '-bis-(2,2,6,6-tetramethyl-4-piperidyl)-1,6-hexamethylene diamine and the chloro-6-of 2,4-bis-(4-morpholinyl)-1,3,5-triazines polymer in one or more combination.
Described aqueous vapor separation layer 2 comprises the raw material of following mass parts: polyvinylidene chloride 70-100 part, inorganic filler 1-20 part, antioxidant 0.5-3 part, anti ultraviolet agent 0.5-3 part.
In described aqueous vapor separation layer 2, inorganic filler is one or more the combination in titanium dioxide, talcum powder, imvite, silica, calcium carbonate.
In described aqueous vapor separation layer 2, antioxidant is 2, 6-di-t-butyl-4-methylphenol, n-octadecane base-3-(3 ', 5 '-two tertiary Ding-4 '-hydroxy phenyl) propionic ester, four-[methylene-3-(3 ', 5 '-di-t-butyl-4-hydroxy phenyl) propionic ester] methane, three (3, 5-di-t-butyl-4-hydroxybenzyl) isocyanuric acid ester, triethylene glycol-bis--[3-(3-tertiary butyl-4-hydroxy-5-aminomethyl phenyl) propionic ester], 2, 2 '-di-2-ethylhexylphosphine oxide-(4-methyl-6-tert-butylphenol, 4-4 '-thiobis-(3-methyl-6-tert-butyl phenol), 4-4 '-butyl is two-and (3-methyl-6-tert-butyl phenol), decanedioic acid two (2, 2, 6, 6-tetramethyl-4-piperidyl) ester, tricresyl phosphite (1, 2, 2, 6, 6-pentamethyl-4-piperidyl) ester, poly-[(1-(β-ethyl)-2, 2, 6, 6-tetramethyl-4-piperidyl) succinic acid], poly-{ [6-[(1, 1, 3, 3-tetramethyl butyl)-imino group]-1, 3, 5-triazine-2, 4-bis-base], [2-(2, 2, 6, 6-tetramethyl-4-piperidyl)-secondary amino]-hexa-methylene-[4-(2, 2, 6, 6-tetramethyl-4-piperidyl)-secondary amino] in one or more combination.
In described aqueous vapor separation layer 2, anti ultraviolet agent is 2-(2-hydroxyl-5-aminomethyl phenyl)-BTA, 2-[2-hydroxyl-3, 5-(a, a-dimethyl-benzyl-) phenyl]-BTA, 2-(2-hydroxyl-{ 3, 5-tert-butyl-phenyl)-BTA, 2-(2-hydroxyl-3, 5-butyl-5-aminomethyl phenyl)-5 chlorobenzotriazoles, 2-(2-hydroxyl-3, 5-tert-butyl-phenyl)-5-chlorobenzotriazole, 2-(2-hydroxyl-3, 5-bis--tertiary pentyl phenyl)-BTA, 2-(2-hydroxyl-5-tert-butyl-phenyl)-BTA, one or more combination in 2-(2-hydroxyl-3-sec-butyl-5-tert-butyl-phenyl)-BTA and 2-(the tertiary octyl phenyl of 2-hydroxyl-5-)-BTA.
A kind of preparation method of high water vapor rejection polyvinylidene difluoride film takes following steps:
Respectively by polyvinylidene fluoride layer and aqueous vapor separation layer raw material after 15-40 DEG C of mixed at high speed, to put in double screw extruder 150-220 DEG C respectively and extrude, obtain the raw material particle of polyvinylidene fluoride layer and aqueous vapor separation layer respectively.
Polyvinylidene fluoride layer and aqueous vapor separation layer raw material particle are put in two extruders respectively, at 180-220 DEG C, carries out melting, plasticizing, extrude and conflux in T-shaped die head, being extruded at 190-210 DEG C by die slot.Extrudate carries out cooling and shaping through the chill roll of-20-10 DEG C, and cooled film heat-treats reply sizing, rolling after trimming through the hot blast drying tunnel of 0-50 DEG C, thus obtains required film.
Embodiment 1
The polyvinylidene difluoride film film thickness that the present embodiment provides is 50 microns, two-layer structure, polyvinylidene fluoride layer 5 microns, internal layer 45 microns.Each rete raw material first mixes in high-speed mixer high speed.Polyvinylidene fluoride layer raw material: Kynoar PVDF65 part, polymethyl methacrylate 0.1 part, titanium dioxide 0.1 part, antioxidant decanedioic acid two (2,2,6,6-tetramethyl-4-piperidyl) ester 0.1 part, anti ultraviolet agent 2-(2-hydroxyl-5-aminomethyl phenyl)-BTA 0.1 part; Aqueous vapor separation layer raw material: polyvinylidene chloride 70 parts, titanium dioxide 1 part, antioxidant 4-4 '-thiobis-(3-methyl-6-tert-butyl phenol) 0.5 part, anti ultraviolet agent 2-(2-hydroxyl-5-aminomethyl phenyl)-BTA 0.5 part.
Respectively by polyvinylidene fluoride layer and aqueous vapor separation layer raw material after 15-40 DEG C of mixed at high speed, to put in double screw extruder 150-220 DEG C respectively and extrude, obtain the raw material particle of polyvinylidene fluoride layer and aqueous vapor separation layer respectively.
Polyvinylidene fluoride layer and aqueous vapor separation layer raw material particle are put in two extruders respectively, at 180-220 DEG C, carries out melting, plasticizing, extrude and conflux in T-shaped die head, being extruded at 190-210 DEG C by die slot.Extrudate carries out cooling and shaping through the chill roll of-20-10 DEG C, and cooled film heat-treats reply sizing, rolling after trimming through the hot blast drying tunnel of 0-50 DEG C, thus obtains high water vapor rejection polyvinylidene difluoride film A.
Embodiment 2
The polyvinylidene difluoride film film thickness that the present embodiment provides is 50 microns, two-layer structure, polyvinylidene fluoride layer 10 microns, aqueous vapor separation layer 40 microns.Each rete raw material first mixes in high-speed mixer high speed.Polyvinylidene fluoride layer raw material: Kynoar PVDF70 part, PMA 2 parts, polymethyl methacrylate 0.4 part, titanium dioxide 2 parts, talcum powder 3 parts, antioxidant decanedioic acid two (2,2,6,6-tetramethyl-4-piperidyl) ester 0.2 part, 2,2 '-di-2-ethylhexylphosphine oxide-(4-methyl-6-tert-butylphenol) 0.2 part, anti ultraviolet agent 2-(2-hydroxyl-3,5-bis--tertiary pentyl phenyl)-BTA 0.3 part, 2-hydroxyl-5-chlorobenzophenone 0.2 part; Aqueous vapor separation layer: polyvinylidene chloride 70 parts, titanium dioxide 1 part, 2 parts, calcium carbonate, antioxidant 2,6-di-t-butyl-4-methylphenol 0.1 part, 4-4 '-thiobis-(3-methyl-6-tert-butyl phenol) 0.4 part, anti ultraviolet agent 2-(2-hydroxyl-5-tert-butyl-phenyl)-BTA 0.2 part, 2-(2-hydroxyl-5-aminomethyl phenyl)-BTA 0.3 part.
Respectively by polyvinylidene fluoride layer and aqueous vapor separation layer raw material after 15-40 DEG C of mixed at high speed, to put in double screw extruder 150-220 DEG C respectively and extrude, obtain the raw material particle of polyvinylidene fluoride layer and aqueous vapor separation layer respectively.
Polyvinylidene fluoride layer and aqueous vapor separation layer raw material particle are put in two extruders respectively, at 180-220 DEG C, carries out melting, plasticizing, extrude and conflux in T-shaped die head, being extruded at 190-210 DEG C by die slot.Extrudate carries out cooling and shaping through the chill roll of-20-10 DEG C, and cooled film heat-treats reply sizing, rolling after trimming through the hot blast drying tunnel of 0-50 DEG C, thus obtains high water vapor rejection polyvinylidene difluoride film B.
Embodiment 3
The polyvinylidene difluoride film film thickness that the present embodiment provides is 50 microns, two-layer structure, polyvinylidene fluoride layer 15 microns, aqueous vapor separation layer 35 microns.Each rete raw material first mixes in high-speed mixer high speed.Polyvinylidene fluoride layer raw material: Kynoar PVDF70 part, PMA 5 parts, polymethyl methacrylate 2 parts, titanium dioxide 2 parts, imvite 6 parts, antioxidant decanedioic acid two (2, 2, 6, 6-tetramethyl-4-piperidyl) ester 0.3 part, triethylene glycol-bis--[3-(3-tertiary butyl-4-hydroxy-5-aminomethyl phenyl) propionic ester] 0.3 part, anti ultraviolet agent 2-(2-hydroxyl-3, 5-bis--tertiary pentyl phenyl)-BTA 0.3 part, 2-hydroxyl-5-chlorobenzophenone 0.2 part, 2, 2 '-dihydroxy-4, 4 '-dimethoxy-benzophenone 0.3 part, aqueous vapor separation layer: polyvinylidene chloride 70 parts, titanium dioxide 1 part, talcum powder 12 parts, antioxidant 2,6-di-t-butyl-4-methylphenol 0.2 part, 4-4 '-thiobis-(3-methyl-6-tert-butyl phenol) 0.4 part, anti ultraviolet agent 2-(2-hydroxyl-5-tert-butyl-phenyl)-BTA 0.3 part, 2-(2-hydroxyl-5-aminomethyl phenyl)-BTA 0.3 part.
Respectively by polyvinylidene fluoride layer and aqueous vapor separation layer raw material after 15-40 DEG C of mixed at high speed, to put in double screw extruder 150-220 DEG C respectively and extrude, obtain the raw material particle of polyvinylidene fluoride layer and aqueous vapor separation layer respectively.
Polyvinylidene fluoride layer and aqueous vapor separation layer raw material particle are put in two extruders respectively, at 180-220 DEG C, carries out melting, plasticizing, extrude and conflux in T-shaped die head, being extruded at 190-210 DEG C by die slot.Extrudate carries out cooling and shaping through the chill roll of-20-10 DEG C, and cooled film heat-treats reply sizing, rolling after trimming through the hot blast drying tunnel of 0-50 DEG C, thus obtains high water vapor rejection polyvinylidene difluoride film B.
Embodiment 4
The polyvinylidene difluoride film film thickness that the present embodiment provides is 50 microns, two-layer structure, polyvinylidene fluoride layer 30 microns, aqueous vapor separation layer 20 microns.Each rete raw material first mixes in high-speed mixer high speed.Polyvinylidene fluoride layer raw material: Kynoar PVDF80 part, PMA 8 parts, polymethyl methacrylate 2 parts, titanium dioxide 2 parts, talcum powder 8 parts, imvite 3 parts, antioxidant decanedioic acid two (2, 2, 6, 6-tetramethyl-4-piperidyl) ester 0.3 part, triethylene glycol-bis--[3-(3-tertiary butyl-4-hydroxy-5-aminomethyl phenyl) propionic ester] 0.3 part, three (3, 5-di-t-butyl-4-hydroxybenzyl) isocyanuric acid ester 1.2 parts, anti ultraviolet agent 2-(2-hydroxyl-3, 5-bis--tertiary pentyl phenyl)-BTA 0.3 part, 2-hydroxyl-5-chlorobenzophenone 0.3 part, 2, 2 '-dihydroxy-4, 4 '-dimethoxy-benzophenone 1.2 parts, aqueous vapor separation layer: polyvinylidene chloride 80 parts, titanium dioxide 2 parts, talcum powder 10 parts, antioxidant 2,6-di-t-butyl-4-methylphenol 0.8 part, 4-4 '-thiobis-(3-methyl-6-tert-butyl phenol) 0.4 part, 2,2 '-di-2-ethylhexylphosphine oxide-(4-methyl-6-tert-butylphenol) 1.2 parts, anti ultraviolet agent 2-(2-hydroxyl-5-tert-butyl-phenyl)-BTA 0.3 part, 2-(2-hydroxyl-5-aminomethyl phenyl)-BTA 0.3 part, 2-(2-hydroxyl-3,5-tert-butyl-phenyl)-5-chlorobenzotriazole 0.2 part.
Respectively by polyvinylidene fluoride layer and aqueous vapor separation layer raw material after 15-40 DEG C of mixed at high speed, to put in double screw extruder 150-220 DEG C respectively and extrude, obtain the raw material particle of polyvinylidene fluoride layer and aqueous vapor separation layer respectively.
Polyvinylidene fluoride layer and aqueous vapor separation layer raw material particle are put in two extruders respectively, at 180-220 DEG C, carries out melting, plasticizing, extrude and conflux in T-shaped die head, being extruded at 190-210 DEG C by die slot.Extrudate carries out cooling and shaping through the chill roll of-20-10 DEG C, and cooled film heat-treats reply sizing, rolling after trimming through the hot blast drying tunnel of 0-50 DEG C, thus obtains high water vapor rejection polyvinylidene difluoride film D.
Embodiment 5
The polyvinylidene difluoride film film thickness that the present embodiment provides is 50 microns, two-layer structure, polyvinylidene fluoride layer 45 microns, aqueous vapor separation layer 5 microns.Each rete raw material first mixes in high-speed mixer high speed.Polyvinylidene fluoride layer raw material: Kynoar PVDF90 part, polyethyl acrylate 8 parts, polyethyl methacrylate 22 parts, titanium dioxide 2 parts, talcum powder 3 parts, imvite 10 parts, antioxidant decanedioic acid two (2,2,6,6-tetramethyl-4-piperidyl) ester 1.5 parts, triethylene glycol-bis--[3-(3-tertiary butyl-4-hydroxy-5-aminomethyl phenyl) propionic ester] 1.5 parts, anti ultraviolet agent 2-(2-hydroxyl-3,5-bis--tertiary pentyl phenyl)-BTA 0.3 part, 2-hydroxyl-5-chlorobenzophenone 2.7 parts; Aqueous vapor separation layer: polyvinylidene chloride 100 parts, titanium dioxide 3 parts, talcum powder 17 parts, antioxidant 2,6-di-t-butyl-4-methylphenol 0.8 part, 4-4 '-thiobis-(3-methyl-6-tert-butyl phenol) 0.2 part, 2,2 '-di-2-ethylhexylphosphine oxide-(4-methyl-6-tert-butylphenol) 2 parts, anti ultraviolet agent 2-(2-hydroxyl-5-tert-butyl-phenyl)-BTA 1 part, 2-(2-hydroxyl-5-aminomethyl phenyl)-BTA 1 part, 2-(2-hydroxyl-3,5-tert-butyl-phenyl)-5-chlorobenzotriazole 1 part.
Respectively by polyvinylidene fluoride layer and aqueous vapor separation layer raw particles after 15-40 DEG C of mixed at high speed, to put in double screw extruder 150-220 DEG C respectively and extrude, obtain the raw material particle of polyvinylidene fluoride layer and aqueous vapor separation layer respectively.
Polyvinylidene fluoride layer and aqueous vapor separation layer raw material particle are put in two extruders respectively, at 180-220 DEG C, carries out melting, plasticizing, extrude and conflux in T-shaped die head, being extruded at 190-210 DEG C by die slot.Extrudate carries out cooling and shaping through the chill roll of-20-10 DEG C, and cooled film heat-treats reply sizing, rolling after trimming through the hot blast drying tunnel of 0-50 DEG C, thus obtains high water vapor rejection polyvinylidene difluoride film E.
Above-mentioned for gained film sample is carried out testing vapor transmission, and comparative sample is the PVDF thin film of 50 microns, and carries out PID test to the solar module encapsulated after this Film laminated backboard of use, and test result is as follows:
Sample Water vapor transmittance: g/ (m 2*24h) Component power attenuation degree (%) after PID test
A 1.1 0.8
B 1.2 1.2
C 1.5 1.3
D 1.6 1.5
E 1.9 1.8
Contrast sample 35 6
Test result illustrates:
Compare than sample PVDF thin film, the film water vapor transmittance that embodiment obtains is all at 2g/ (m 2* 24h) below, use the backboard sample of this Film laminated, carry out PID test after being packaged into solar module, the power attenuation of assembly is all below 2%, and comparative sample power attenuation is 6%.Illustrate the film of the present embodiment can be good obstruct steam, strengthen the anti-PID performance of assembly.

Claims (14)

1. a high water vapor rejection polyvinylidene difluoride film, is characterized in that: comprise polyvinylidene fluoride layer and aqueous vapor separation layer, and the side of described polyvinylidene fluoride layer is compounded with aqueous vapor separation layer.
2. a kind of high water vapor rejection polyvinylidene difluoride film according to claim 1, is characterized in that: high water vapor rejection polyvinylidene difluoride film adopts thermoplastic mode that is multi-layer co-extruded or the common blown film of multilayer to prepare.
3. a kind of high water vapor rejection polyvinylidene difluoride film according to claim 1, is characterized in that: the thickness of described polyvinylidene fluoride layer is 5-45 micron, and described water vapor rejection layer thickness is 5-45 micron.
4. the preparation method of a kind of high water vapor rejection polyvinylidene difluoride film according to claim 1, is characterized in that: take following steps:
Respectively by polyvinylidene fluoride layer and aqueous vapor separation layer raw material after 15-40 DEG C of mixed at high speed, to put in double screw extruder 150-220 DEG C respectively and extrude, obtain the raw material particle of polyvinylidene fluoride layer and aqueous vapor separation layer respectively;
Polyvinylidene fluoride layer and aqueous vapor separation layer raw material particle are put in two extruders respectively, at 180-220 DEG C, carries out melting, plasticizing, extrude and conflux in T-shaped die head, being extruded at 190-210 DEG C by die slot;
Extrudate carries out cooling and shaping through the chill roll of-20-10 DEG C, and cooled film heat-treats reply sizing, rolling after trimming through the hot blast drying tunnel of 0-50 DEG C, thus obtains required high water vapor rejection polyvinylidene difluoride film.
5. the preparation method of a kind of high water vapor rejection polyvinylidene difluoride film according to claim 4, is characterized in that:
Described polyvinylidene fluoride layer comprises the raw material of following mass parts: Kynoar 60-90 part, plasticity resin 0.1-30 part, inorganic filler 0.1-15 part, antioxidant 0.1-3 part, anti ultraviolet agent 0.1-3 part.
6. the preparation method of a kind of high water vapor rejection polyvinylidene difluoride film according to claim 5, it is characterized in that: described Kynoar molecular weight is 20-100 ten thousand, molecular weight distribution width is 1.1-2.
7. the preparation method of a kind of high water vapor rejection polyvinylidene difluoride film according to claim 5, is characterized in that: described plasticity resin is one or more the combination in esters of acrylic acid, methacrylate-based resin class.
8. the preparation method of a kind of high water vapor rejection polyvinylidene difluoride film according to claim 5, is characterized in that: in described polyvinylidene fluoride layer, inorganic filler is one or more the combination in titanium dioxide, talcum powder, silica, imvite.
9. the preparation method of a kind of high water vapor rejection polyvinylidene difluoride film according to claim 5, it is characterized in that: in described polyvinylidene fluoride layer, antioxidant is three (3, 5-di-t-butyl-4-hydroxybenzyl) isocyanuric acid ester, triethylene glycol-bis--[3-(3-tertiary butyl-4-hydroxy-5-aminomethyl phenyl) propionic ester], 2, 2 '-di-2-ethylhexylphosphine oxide-(4-methyl-6-tert-butylphenol, 4-4 '-thiobis-(3-methyl-6-tert-butyl phenol), 4-4 '-butyl is two-and (3-methyl-6-tert-butyl phenol), decanedioic acid two (2, 2, 6, 6-tetramethyl-4-piperidyl) ester, tricresyl phosphite (1, 2, 2, 6, 6-pentamethyl-4-piperidyl) ester, poly-[(1-(β-ethyl)-2, 2, 6, 6-tetramethyl-4-piperidyl) succinic acid], poly-{ [6-[(1, 1, 3, 3-tetramethyl butyl)-imino group]-1, 3, 5-triazine-2, 4-bis-base], [2-(2, 2, 6, 6-tetramethyl-4-piperidyl)-secondary amino]-hexa-methylene-[4-(2, 2, 6, 6-tetramethyl-4-piperidyl)-secondary amino] in one or more combination.
10. the preparation method of a kind of high water vapor rejection polyvinylidene difluoride film according to claim 5, is characterized in that: in described polyvinylidene fluoride layer, anti ultraviolet agent is 2,2 '-dihydroxy-4,4 '-dimethoxy-benzophenone, 2-hydroxyl-5-chlorobenzophenone, 2-(2 '-hydroxyl-5 '-tert-butyl-phenyl) BTA, 2-(2 '-hydroxyl-5 '-aminophenyl) BTA, salicyl salicylate (salsalate) bisphenol-A ester, 2-(2-hydroxyl-3,5-di-tert-pentyl-phenyl) BTA, 2,2 '-(Isosorbide-5-Nitrae-phenylene) two-4H-3,1-benzoxazine-4-ketone, 2-(2 '-hydroxyl-3 ', 5 '-3,5-dimethylphenyl) BTA, 2-(2 '-methyl-4 '-hydroxy phenyl) BTA, two-(2-methoxyl group-4-hydroxyl-5-benzoylphenyl) methane, 2-(2 '-hydroxy-5-methyl base phenyl) BTA, 2-(2 '-hydroxyl-5-aminomethyl phenyl)-5-butyl ester BTA, 2-hydroxyl-4-alkoxy benzophenone, 3,5-di-t-butyl-4-hydroxyl-benzoic acid cetyl ester, three (1,2,2,6,6-pentamethyl-4-piperidyl) phosphite ester, two-2,2,6, the 6-tetramethyl piperidine alcohol esters of decanedioic acid, the polymer of succinic acid and 4-hydroxyl-2,2,6,6-tetramethyl-1-piperidine alcohols, N, N ' polymer of amino-1,3, the 5-triazine of-bis-(2,2,6,6-tetramethyl-4-piperidyl)-1,6-hexamethylene diamine and the chloro-6-of 2,4-bis-(1,1,3,3-tetramethyl butyl), N, N '-bis-(2,2,6,6-tetramethyl-4-piperidyl)-1,6-hexamethylene diamine and the chloro-6-of 2,4-bis-(4-morpholinyl)-1,3,5-triazines polymer in one or more combination.
The preparation method of 11. a kind of high water vapor rejection polyvinylidene difluoride films according to claim 4, it is characterized in that: described aqueous vapor separation layer comprises the raw material of following mass parts: polyvinylidene chloride 70-100 part, inorganic filler 1-20 part, antioxidant 0.5-3 part, anti ultraviolet agent 0.5-3 part.
The preparation method of 12. a kind of high water vapor rejection polyvinylidene difluoride films according to claim 11, is characterized in that: in described aqueous vapor separation layer, inorganic filler is one or more the combination in titanium dioxide, talcum powder, imvite, silica, calcium carbonate.
The preparation method of 13. a kind of high water vapor rejection polyvinylidene difluoride films according to claim 11, it is characterized in that: in described aqueous vapor separation layer, antioxidant is 2, 6-di-t-butyl-4-methylphenol, n-octadecane base-3-(3 ', 5 '-two tertiary Ding-4 '-hydroxy phenyl) propionic ester, four-[methylene-3-(3 ', 5 '-di-t-butyl-4-hydroxy phenyl) propionic ester] methane, three (3, 5-di-t-butyl-4-hydroxybenzyl) isocyanuric acid ester, triethylene glycol-bis--[3-(3-tertiary butyl-4-hydroxy-5-aminomethyl phenyl) propionic ester], 2, 2 '-di-2-ethylhexylphosphine oxide-(4-methyl-6-tert-butylphenol, 4-4 '-thiobis-(3-methyl-6-tert-butyl phenol), 4-4 '-butyl is two-and (3-methyl-6-tert-butyl phenol), decanedioic acid two (2, 2, 6, 6-tetramethyl-4-piperidyl) ester, tricresyl phosphite (1, 2, 2, 6, 6-pentamethyl-4-piperidyl) ester, poly-[(1-(β-ethyl)-2, 2, 6, 6-tetramethyl-4-piperidyl) succinic acid], poly-{ [6-[(1, 1, 3, 3-tetramethyl butyl)-imino group]-1, 3, 5-triazine-2, 4-bis-base], [2-(2, 2, 6, 6-tetramethyl-4-piperidyl)-secondary amino]-hexa-methylene-[4-(2, 2, 6, 6-tetramethyl-4-piperidyl)-secondary amino] in one or more combination.
The preparation method of 14. a kind of high water vapor rejection polyvinylidene difluoride films according to claim 11, it is characterized in that: in described aqueous vapor separation layer, anti ultraviolet agent is 2-(2-hydroxyl-5-aminomethyl phenyl)-BTA, 2-[2-hydroxyl-3, 5-(a, a-dimethyl-benzyl-) phenyl]-BTA, 2-(2-hydroxyl-{ 3, 5-tert-butyl-phenyl)-BTA, 2-(2-hydroxyl-3, 5-butyl-5-aminomethyl phenyl)-5 chlorobenzotriazoles, 2-(2-hydroxyl-3, 5-tert-butyl-phenyl)-5-chlorobenzotriazole, 2-(2-hydroxyl-3, 5-bis--tertiary pentyl phenyl)-BTA, 2-(2-hydroxyl-5-tert-butyl-phenyl)-BTA, one or more combination in 2-(2-hydroxyl-3-sec-butyl-5-tert-butyl-phenyl)-BTA and 2-(the tertiary octyl phenyl of 2-hydroxyl-5-)-BTA.
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CN103832038A (en) * 2014-03-07 2014-06-04 江苏昊华光伏科技有限公司 Black infrared reflection polyvinylidene fluoride (PVDF) solar cell rear panel composite film and manufacturing method thereof
CN204749424U (en) * 2015-05-18 2015-11-11 中天科技精密材料有限公司 High steam separation polyvinylidene fluoride film

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CN106366519A (en) * 2016-09-19 2017-02-01 浙江凯阳新材料股份有限公司 Polyvinylidene fluoride thin film and preparing method thereof
CN106541656A (en) * 2016-09-19 2017-03-29 浙江凯阳新材料股份有限公司 It is a kind of it is three-layer co-extruded go out polyvinylidene difluoride film and preparation method thereof
CN111763393A (en) * 2020-05-28 2020-10-13 中裕软管科技股份有限公司 High-air-tightness PVDF (polyvinylidene fluoride) base material special for oilfield restoration pipe and preparation method thereof
CN113232340A (en) * 2021-03-24 2021-08-10 浙江大东南股份有限公司 Preparation method of white hydrolysis-resistant anti-aging BOPET (biaxially-oriented polyethylene terephthalate) back plate film

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